6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS
FDA 510(k)
FDA Class 2
·General Hospital
BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER
FDA 510(k)
FDA Class 2
·Orthopedic
VALIDATE D-Dimer Calibration Verification / Linearity Test Kit
FDA 510(k)
FDA Class 2
·Hematology
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 26, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
JUMAO MEDICAL EQUIPMENT·Product code IOR·July 31, 2014